- Senior Regulatory Program Manager Oncology
The Program Manager position will be responsible for regional (EU, ROW) regulatory strategic and operational management of a project, , or a portfolio of projects
Primary Responsibilities and Accountabilities
Is responsible for and leads the development and implementation of regional regulatory strategies on projects
Gives regional strategic regulatory input to the RAFT and Project Teams for lifecycle management of products
Analyzes regulatory environment for impact on projec ...
- PW 6429 Manager Regulatory Affairs- Immunology
This is an excellent opportunity for an experienced regulatory professional to join our top global pharmaceutical client’s team working specifically on their Immunology portfolio. You will be responsible for Phase II / III projects, ultimately resulting in MAA preparation and filing. This company offers fantastic career development opportunities and exposure to an exciting product portfolio.
- Associate Director, EU Regulatory Affairs Strategy Oncology
I am currently partnering with an innovative, mid-sized company within the biopharmaceutical arena. This company are recruiting for a new position within their European Regulatory Affairs team due to the large amount of new clinical development programs they are running within Oncology. This role is offered at ‘Associate Director’ level and will cover the European region for Oncology.
- Project Lead - Labelling - Home-based
Labelling project manager – Home-basedThe companyThis company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
- Regulatory Affairs Director (GRL) for Oncology Franchise - Based in Central (West) London – Medium Sized Pharma with strong Pipeline
Take strategic ownership of an early phase development portfolio for NME’s in both Oncology and CNS & Have a big impact on a developing regulatory department, where you can lead and mentor a number of talented and motivated regulatory professionals...!!! If you wish to apply for this role send your CV to firstname.lastname@example.org or call Theo Moore or Matt Grieg in the London office on +44 (0)207 801 3380 -
- PW 6346 European Study Manager – Oncology
An excellent opportunity for an experienced Lead CRA/ Associate Study Manager, with EU monitoring or trial management experience to join a leading Oncology biotech. You will be responsible for the management and co-ordination of EU trials with full oversight of required vendors. This is a pivotal role within an organisation who has received global recognition for their diverse portfolio. The role will start early in January, interviews to take place October.
- Senior Clinical Project Manager (SCPM) - Oncology
Newly created position for a Senior Clinical Project Manager. I am looking for a home or office based Senior Clinical Project Manager (SCPM) to be based in any European Country. Reporting into the European Head of Project Management.
- Senior Clinical Project Manager -Oncology - Eastern / Central Europe
Newly created position for a Senior Clinical Project Manager for Eastern / Central Europe with a focus on Oncology Trials. I am looking for a home or office based Senior Clinical Project Manager (SCPM) to be based in any Central or Eastern European Country. Reporting into the European Head of Project Management.
- Senior Consultant - Labelling - Home-based
Project Lead – Labelling - Homebased The companyThis company is a top 5 global CRO with a large and ever growing consulting arm. This company is global company with over 10,000 employees across all continents. They are a company that help their clients get medicines into the hands of those who need them most. They offer scientific know how, industry expertise and an outstanding environment to learn and grow. ...
- PW 6425 Clinical Study Manager, Oncology
Excellent opportunity available for an experienced Study Manager/ Clinical Study Manager to join one of our smaller, global pharmaceutical clients. The ideal candidate for this position will hold an extensive Oncology background and would have worked on international studies looking to gain Clinical Project Management experience within pharma. EU candidates open to a move to the UK are also encouraged to apply.